bigdye labeled dye-terminator chemistry (Thermo Fisher)
90
Structured Review
Thermo Fisher
bigdye labeled dye-terminator chemistry
Bigdye Labeled Dye Terminator Chemistry, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dye-labeled+terminators/pmc01277808-45-12-16
Average 90 stars, based on 1 article reviews
Bigdye Labeled Dye Terminator Chemistry, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dye-labeled+terminators/pmc01277808-45-12-16
Average 90 stars, based on 1 article reviews
bigdye labeled dye-terminator chemistry - by Bioz Stars,
2026-10
90/100 stars
Images
Related Articles
Sequencing:Article Title: A survey of Rhipicephalus microplus populations for mutations associated with pyrethroid resistance. Article Snippet: Mutations associated with pyrethroid resistance were found in Mexican strains of Rhipicephalus microplus (Canestrini).. A mutation in the sodium channel gene was reported in strains highly resistant to permethrin and another mutation in an esterase gene in a strain that shows moderate resistance to the same pesticide.. Methods based on the melting temperature difference of ampliÞed allele-speciÞc DNA fragments were developed that can detect these mutations rapidly in individual larvae. Article Title: Multigene phylogenetic and population differentiation data confirm the existence of a cryptic species within Chrysoporthe cubensis. Article Snippet: .. PCR products were sequenced using Article Title: Accounting for female reproductive cycles in a superpopulation capture-recapture framework. Article Snippet: Briefly, the primers dlp1.5 (Baker et al. 1998) and tphe (Carroll et al. 2011a), both modified with a 50-M13 primer extension to facilitate subsequent sequencing reactions, were used to amplify ;950 bp of the mtDNA control region. .. PCR products were purified for sequencing with ExoSAP-IT (USB, Cleveland, Ohio, USA) and sequenced using Article Title: Porcine kallikrein gene family: genomic structure, mapping, and differential expression analysis. Article Snippet: .. The PCR products generated through vectorette PCR were treated with shrimp alkaline phosphatase (1 U μl−1) and Exonuclease III (10 U μl−1) at a volume equaling 5% of the PCR product and incubated at 37 °C for 30 min followed by 80 °C for 10 min. Sequencing reactions were performed in a 10-μl reaction volume containing 2 μl PCR product, 1 mM sequencing primer, 2 μl of other:Article Title: A single catalytic domain of the junction-resolving enzyme T7 endonuclease I is a non-specific nicking endonuclease Article Snippet: DNA sequencing was performed on Article Title: Novel COL4A5, COL4A4, and COL4A3 mutations in Alport syndrome. Article Snippet: For direct sequencing, the Polymerase Chain Reaction:Article Title: Multigene phylogenetic and population differentiation data confirm the existence of a cryptic species within Chrysoporthe cubensis. Article Snippet: .. PCR products were sequenced using Article Title: Accounting for female reproductive cycles in a superpopulation capture-recapture framework. Article Snippet: Briefly, the primers dlp1.5 (Baker et al. 1998) and tphe (Carroll et al. 2011a), both modified with a 50-M13 primer extension to facilitate subsequent sequencing reactions, were used to amplify ;950 bp of the mtDNA control region. .. PCR products were purified for sequencing with ExoSAP-IT (USB, Cleveland, Ohio, USA) and sequenced using Article Title: Porcine kallikrein gene family: genomic structure, mapping, and differential expression analysis. Article Snippet: .. The PCR products generated through vectorette PCR were treated with shrimp alkaline phosphatase (1 U μl−1) and Exonuclease III (10 U μl−1) at a volume equaling 5% of the PCR product and incubated at 37 °C for 30 min followed by 80 °C for 10 min. Sequencing reactions were performed in a 10-μl reaction volume containing 2 μl PCR product, 1 mM sequencing primer, 2 μl of Purification:Article Title: Accounting for female reproductive cycles in a superpopulation capture-recapture framework. Article Snippet: Briefly, the primers dlp1.5 (Baker et al. 1998) and tphe (Carroll et al. 2011a), both modified with a 50-M13 primer extension to facilitate subsequent sequencing reactions, were used to amplify ;950 bp of the mtDNA control region. .. PCR products were purified for sequencing with ExoSAP-IT (USB, Cleveland, Ohio, USA) and sequenced using DNA Extraction:Article Title: G protein-coupled receptor-like receptors and modulators thereof Article Snippet: PCR products were typically gel-purified using QIAquick columns (Qiagen, Valencia, Calif.) and either cloned directly into pCR3.1 (Invitrogen, Carlsbad, Calif.), or indirectly through an initial cloning step into pCR2.1. .. Plasmids containing the appropriate inserts were prepared by a mini-prep DNA isolation procedure (Qiagen) and were sequenced using Generated:Article Title: Porcine kallikrein gene family: genomic structure, mapping, and differential expression analysis. Article Snippet: .. The PCR products generated through vectorette PCR were treated with shrimp alkaline phosphatase (1 U μl−1) and Exonuclease III (10 U μl−1) at a volume equaling 5% of the PCR product and incubated at 37 °C for 30 min followed by 80 °C for 10 min. Sequencing reactions were performed in a 10-μl reaction volume containing 2 μl PCR product, 1 mM sequencing primer, 2 μl of Incubation:Article Title: Porcine kallikrein gene family: genomic structure, mapping, and differential expression analysis. Article Snippet: .. The PCR products generated through vectorette PCR were treated with shrimp alkaline phosphatase (1 U μl−1) and Exonuclease III (10 U μl−1) at a volume equaling 5% of the PCR product and incubated at 37 °C for 30 min followed by 80 °C for 10 min. Sequencing reactions were performed in a 10-μl reaction volume containing 2 μl PCR product, 1 mM sequencing primer, 2 μl of Recombinant:Article Title: G protein-coupled receptor-like receptors and modulators thereof Article Snippet: .. Analysis of the GPCR-Like Receptor Sequences DNA from pCR2.1 recombinant plasmids containing the expected insert size were sequenced using |